Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Brattle Instrument Corp. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Apr 10, 1981: SYNCHRONIZER #208.
| Apr 10, 1981 | SYNCHRONIZER #208K810588 · IXO | 510(k) clearances |
| Feb 2, 1981 | TRANSCUTANEOUS BLOOD OXYGEN MONITOR #300K802978 · KLK | 510(k) clearances |
| Oct 17, 1978 | PHIPIOLOGICAL SYNCHRONIZER PART#205K781681 · IXQ | 510(k) clearances |
| Apr 26, 1977 | MONITOR, FETAL, NO. L04-1100K770692 · HGM | 510(k) clearances |
| Mar 9, 1977 | FETAL MONITOR, PART #101-11009K770296 · HGM | 510(k) clearances |
| Mar 9, 1977 | FETAL MONITOR, PART #100-11009K770297 · HGM | 510(k) clearances |
| Mar 9, 1977 | ABDOMINAL ECG PROCESSOR FOR FETAL MONI.K770295 · HGI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
